The Effect of Transcutaneous Electrical Nerve Stimulation on Pain During Venous Cannulation

Not Applicable

Completed

• Conditions: Cannulation Pain

• Registration Number: NCT01607463
• Lead Sponsor: Kyungpook National University Hospital

Brief Summary

The purpose of this study was to investigate whether transcutaneous electrical nerve stimulation (TENS) could reduce pain during cannulation of vein.

Detailed Description

One hundred patients were allocated randomly to two groups: In the active TENS group TENS was delivered via two electrodes on the venous cannulation site (radial side of the wrist of dominant forearm) 20 min prior to venous cannulation and control group received placebo (no current) TENS. Venous cannulation with a 22 gage cannula was performed. During venous cannulation the pain intensity (0 = no pain, 10 = worst pain imaginable) was measured. Any side effects during study periods were recorded

Study Timeline

• Status Verified: 2012-05
• Study Start: 2012-05
• Primary Completion: 2012-05
• Study Completion: 2012-05
• Study First Submitted: 2012-05-22
• Study First Submitted QC: 2012-05-24
• Last Update Submitted: 2012-05-24
• Study First Posted: 2012-05-30
• Last Update Posted: 2012-05-30

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 100

Inclusion Criteria

• outpatients who underwent plastic surgery

Exclusion Criteria

• concomitant sedative or analgesic medication,
• neurological disease.
• all patients with potentially dangerous internal diseases (American Society of Anesthesiologists' physical status > 3).

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: FACTORIAL

Primary Outcome Measures

Name	Time	Method
The effect of transcutaneous electrical nerve stimulation on pain during venous cannulation	one minute after cannulation	One hundred patients were allocated randomly to two groups: In the active TENS group TENS was delivered via two electrodes on the venous cannulation site (radial side of the wrist of dominant forearm) 20 min prior to venous cannulation and control group received placebo (no current) TENS. Venous cannulation with a 22 gage cannula was performed. One minute after venous cannulation the pain intensity (0 = no pain, 10 = worst pain imaginable) was measured. Any side effects during study periods were recorded